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155505-55-8

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155505-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155505-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,0 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155505-55:
(8*1)+(7*5)+(6*5)+(5*5)+(4*0)+(3*5)+(2*5)+(1*5)=128
128 % 10 = 8
So 155505-55-8 is a valid CAS Registry Number.

155505-55-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl 2-[4-(hydroxymethyl)phenoxy]acetate

1.2 Other means of identification

Product number -
Other names allyl 2-(4-hydroxymethylphenoxy)acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:155505-55-8 SDS

155505-55-8Relevant articles and documents

Internal resin capture - A self purification method for the synthesis of C-terminally modified peptides

Davies, Michael,Bradley, Mark

, p. 4733 - 4746 (1999)

A synthetic strategy which allows for the general modification of peptides at the C-terminus has long been the goal of the synthetic chemist. We report here the full synthetic details of our inversion and modification methodology demonstrating the method with the synthesis of peptide amides, alcohols, nitriles and a range of other modified peptides.

Optimising inhibitors of trypanothione reductase using solid-phase chemistry

Chitkul, Bordin,Bradley, Mark

, p. 2367 - 2369 (2007/10/03)

A series of inhibitors of the enzyme trypanothione reductase has been identified using directed solid-phase chemistry. The compounds were based on a series of polyamine scaffolds and used the natural product kukoamine A as the lead structure. A compound with a K(i) of 76 nM was identified, although somewhat surprisingly the compound appeared to be noncompetitive in nature. (C) 2000 Elsevier Science Ltd.

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